University of Veterinary Medicine Vienna, Vienna, Austria.
Center for Physiology and Pharmacology, Medical University of Vienna, Vienna, Austria.
Biomed Pharmacother. 2024 Aug;177:117057. doi: 10.1016/j.biopha.2024.117057. Epub 2024 Jul 7.
Cyclotides are head-to-tail cyclized peptides with a unique cystine-knot motif. Their structure provides exceptional resistance against enzymatic, chemical, or thermal degradation compared to other peptides. Peptide-based therapeutics promise high specificity, selectivity and lower immunogenicity, making them safer alternatives to small molecules or large biologicals. Cyclotides were researched due to their anti-cancer properties by inducing apoptosis in tumor cells in the past, but the impact of cyclotides on cytotoxic immune cells was poorly studied. Natural Killer (NK) cells are cytotoxic innate lymphoid cells and play an important role in the defense against infected, stressed and transformed cells. NK cells do not need prior sensitization and act in an antigen independent manner, holding promising potential in the field of immunotherapy. To investigate the effect of immunomodulatory cyclotides on NK cells, we evaluated several peptide-enriched plant extracts on NK cell mediated cytotoxicity. We observed that the extract samples derived from Carapichea ipecacuanha (Brot.) L. Andersson augments the killing potential of mouse NK cells against different tumor targets in vitro. Subsequent isolation of cyclotides from C. ipecacuanha extracts led to the identification of a primary candidate that enhances cytotoxicity of both mouse and human NK cells. The augmented killing is facilitated by the increased degranulation capacity of NK cells. In addition, we noted a direct toxic effect of caripe 8 on tumor cells, suggesting a dual therapeutic potential in cancer treatment. This study offers novel insights how natural peptides can influence NK cell cytotoxicity. These pre-clinical findings hold significant promise for advancing current immunotherapeutic approaches.
环肽是具有独特半胱氨酸结基序的头尾环化肽。与其他肽相比,其结构提供了对酶、化学或热降解的非凡抗性。基于肽的疗法具有高特异性、选择性和较低的免疫原性,使其成为小分子或大型生物制剂的更安全替代品。过去,环肽因其具有抗癌特性而被研究,可诱导肿瘤细胞凋亡,但环肽对细胞毒性免疫细胞的影响研究甚少。自然杀伤 (NK) 细胞是细胞毒性先天淋巴细胞,在防御感染、应激和转化细胞方面发挥着重要作用。NK 细胞不需要预先致敏,以非抗原依赖的方式发挥作用,在免疫治疗领域具有很大的应用潜力。为了研究免疫调节环肽对 NK 细胞的影响,我们评估了几种富含肽的植物提取物对 NK 细胞介导的细胞毒性的影响。我们观察到,来自 Carapichea ipecacuanha (Brot.) L. Andersson 的提取物样品增强了体外小鼠 NK 细胞对不同肿瘤靶标的杀伤潜力。随后从 C. ipecacuanha 提取物中分离出环肽,鉴定出一种增强小鼠和人 NK 细胞细胞毒性的主要候选物。NK 细胞脱颗粒能力的增加促进了杀伤作用。此外,我们注意到 caripe 8 对肿瘤细胞有直接的毒性作用,提示其在癌症治疗中有双重治疗潜力。这项研究提供了关于天然肽如何影响 NK 细胞细胞毒性的新见解。这些临床前发现为推进当前的免疫治疗方法提供了重要的前景。